dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 809087311000119106

Production

add

Component

809087311000119106

The component that hold information about this concept.

Fully Specified Name (FSN)

Carrier of nebulin-related nemaline myopathy (finding)

Shortest Term

Carrier of neb-related nemaline myopathy

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Carrier of nebulin-related nemaline myopathy (finding)

SCTID: 809087311000119106, Primitive, Active

809087311000119106|Carrier of nebulin-related nemaline myopathy (finding)|

vi Người mang bệnh loạn dưỡng cơ nebulin liên quan đến nemaline (phát hiện)
en Carrier of neb-related nemaline myopathy
en Carrier of nebulin-related nemaline myopathy
en Carrier of nebulin-related nemaline myopathy (finding)

Expression

809087311000119106 |Carrier of nebulin-related nemaline myopathy (finding)|
 <<< 47461006 |Genetic disorder carrier (finding)| : 
        { 363714003 |Interprets (attribute)| = 278844005 |General clinical state (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
2006421 - Người mang bệnh loạn dưỡng cơ Nebulin liên quan đến Nemaline (phát hiện) (vi) View
2006421	vi	Synonym (core metadata concept)	Người mang bệnh loạn dưỡng cơ Nebulin liên quan đến Nemaline (phát hiện)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5198383015 - Carrier of NEB-related nemaline myopathy (en) View
5198383015	en	Synonym (core metadata concept)	Carrier of NEB-related nemaline myopathy	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
5223682012 - Carrier of Nebulin-related nemaline myopathy (en) View
5223682012	en	Synonym (core metadata concept)	Carrier of Nebulin-related nemaline myopathy	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
5198384014 - Carrier of Nebulin-related nemaline myopathy (finding) (en) View
5198384014	en	Fully specified name (core metadata concept)	Carrier of Nebulin-related nemaline myopathy (finding)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15588055022) - 809087311000119106 -> 47461006 (116680003) View
116680003 \|Is a (attribute)\|	47461006 \|Genetic disorder carrier (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15588056023) - 809087311000119106 -> 278844005 (363714003) View
363714003 \|Interprets (attribute)\|	278844005 \|General clinical state (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
47461006 View
47461006	Genetic disorder carrier (finding)	Genetic disorder carrier	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (bafe8d3a-c0cf-594c-99cd-4fe1b24881a2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|

Terminology chevron_right Concepts chevron_right 809087311000119106

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches